Details Top

Internal ID UUID68f91e89e4b60036166157
Scientific name Tecomaria capensis
Authority (Thunb.) Spach
First published in Hist. Nat. Vég. 9: 137 (1840)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Ornamental horticulture: cultivated widely as a garden ornamental; used as a climbing vine, shrub, hedge, or groundcover; valued for its bright orange tubular flowers and year‑round bloom in subtropical and tropical climates.
- Cut‑flower trade: occasionally harvested as a cut flower for local and regional floral arrangements; stems bearing open blossoms are marketed locally in South Africa and occasionally supplied to regional floral markets.
- Landscaping and erosion control: employed in public and private landscaping, especially for xeriscaping and ecological restoration projects because of its rapid growth and pollinator support.

Food and beverages (non‑medicinal):
- Nectar source for honey production: the abundant tubular flowers provide nectar for honeybees and other pollinators; the nectar contributes to honey production, and some local beekeepers market honey derived from this source.

Properties relevant to use:
- Evergreen shrub with climbing habit; reaches 3–5 m in height.
- Thrives in full sun to partial shade, tolerates drought, and adapts to a range of soils.
- Continuous floral display in favorable climates; high nectar production attracts sunbirds (Nectarina spp.) in its native range and hummingbirds where introduced.
- Non‑woody stems make it unsuitable for timber, but vigorous growth enables easy propagation by cuttings.

Standards and regulation:
- Not listed in the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
- International trade is subject to national plant‑health regulations (e.g., EU Phytosanitary Directive 2000/29/EC; US Department of Agriculture APHIS rules).
- No specific product standards exist for the ornamental plant; trade follows general horticultural certification schemes.

Sustainability and sourcing:
- Propagated mainly by vegetative cuttings; low genetic selection pressure.
- Cultivated on commercial nurseries in South Africa, the United States (Florida, California), and other subtropical regions; wild harvest is negligible.
- Considered low risk for invasion; naturalized populations are monitored but not classified as high‑impact invasive species in most jurisdictions.
- Sustainable horticultural production relies on standard nursery practices and integrated pest management.

Synonyms Top

Scientific name Authority First published in
Tecoma petersii Klotzsch Naturw. Reise Mossambique 6(1): 193 (1861)
Tecomaria krebsii Klotzsch Naturw. Reise Mossambique 6(1): 193 (1861)
Tecomaria petersii Klotzsch Naturw. Reise Mossambique 6(1): 192 (1861)
Bignonia capensis Thunb. Prodr. Pl. Cap. : 105 (1794)
Ducoudraea capensis Bureau Monogr. Bignon. : 49 (1864)
Gelseminum capense Kuntze Revis. Gen. Pl. 2: 479 (1891)
Tecomaria capensis var. flava Verdc. Fl. Trop. E. Africa , Bignoniac. & Cobaeac.: 25 (2006)
Tecoma capensis (Thunb.) Lindl. Bot. Reg. 13: t. 1117 (1828)

Common names Top

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Language Common/alternative name
English cape honeysuckle
Afrikaans kaapse kanferfoelie
Arabic تيكومة رأس الرجاء
Arabic تيكوماريا كابينسيس
Bengali লাল চন্দ্রপ্রভা
French chèvrefeuille du cap
Hebrew טקומית
Hebrew טקומית הכף
Japanese ヒメノウゼンカズラ
Russian Текома капская
Swedish kaptrumpet
Vietnamese Đăng tiêu đứng
Chinese 硬骨凌霄
Chinese 铁角凌霄
Chinese 鐵角凌霄

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
Florida Plant Atlas 330
USDA Plants TECA8
Tropicos 3700906
INPN 125819
KEW urn:lsid:ipni.org:names:111129-1
The Plant List kew-318839
Nature Serve 2.135757
IUCN Red List 82858988
IPNI 111129-1
iNaturalist 141858
GBIF 3172489
Freebase /m/02pw_lt
EPPO TEOCA
EOL 484626
Calflora (Californian flora) 9419
USDA GRIN 80086
Wikipedia Tecoma_capensis
Open Tree Of Life 763804
World Flora Online wfo-0000779994
Tropicos 3700026
Flora of Italy 8630
KEW urn:lsid:ipni.org:names:111333-1
Open Tree Of Life 763804
Observations.org 199622
NCBI Taxonomy 140035
IPNI 111333-1
iNaturalist 286772
GBIF 3172490
USDA GRIN 80118
Wikipedia Tecomaria_capensis

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Use of Medicinal Plants in the Process of Wound Healing: A Literature Review Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL Pharmaceuticals (Basel) 27-Feb-2024
PMCID:PMC10975678
doi:10.3390/ph17030303
PMID:38543089
Monstera deliciosa mediated single step biosynthesis of gold nanoparticles by bottom-up approach and its non-antimicrobial properties Shirsul J, Tripathi A, Mohanta D, Ankamwar B 3 Biotech 18-Jan-2024
PMCID:PMC10796889
doi:10.1007/s13205-023-03898-0
PMID:38261935
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
The complete plastome of Campsis radicans (L.) Bureau 1864 and its phylogenetic analysis Li H, Wang L, Ma C Mitochondrial DNA B Resour 07-Nov-2023
PMCID:PMC10796121
doi:10.1080/23802359.2023.2275827
PMID:38239913
Current Overview of Metal Nanoparticles’ Synthesis, Characterization, and Biomedical Applications, with a Focus on Silver and Gold Nanoparticles Burlec AF, Corciova A, Boev M, Batir-Marin D, Mircea C, Cioanca O, Danila G, Danila M, Bucur AF, Hancianu M Pharmaceuticals (Basel) 04-Oct-2023
PMCID:PMC10610223
doi:10.3390/ph16101410
PMID:37895881
Endophytic fungi mediates production of bioactive secondary metabolites via modulation of genes involved in key metabolic pathways and their contribution in different biotechnological sector Toppo P, Kagatay LL, Gurung A, Singla P, Chakraborty R, Roy S, Mathur P 3 Biotech 14-May-2023
PMCID:PMC10183385
doi:10.1007/s13205-023-03605-z
PMID:37197561
An inventory of native-alien populations in South Africa Nelufule T, Robertson MP, Wilson JR, Faulkner KT Sci Data 15-Apr-2023
PMCID:PMC10105770
doi:10.1038/s41597-023-02119-w
PMID:37061528
Current Trends and Prospects for Application of Green Synthesized Metal Nanoparticles in Cancer and COVID-19 Therapies Mbatha LS, Akinyelu J, Chukwuma CI, Mokoena MP, Kudanga T Viruses 13-Mar-2023
PMCID:PMC10054370
doi:10.3390/v15030741
PMID:36992450
Meloidogyne enterolobii risk to agriculture, its present status and future prospective for management Sikandar A, Jia L, Wu H, Yang S Front Plant Sci 24-Jan-2023
PMCID:PMC9902769
doi:10.3389/fpls.2022.1093657
PMID:36762171
A Comprehensive Review of Natural Compounds for Wound Healing: Targeting Bioactivity Perspective Trinh XT, Long NV, Van Anh LT, Nga PT, Giang NN, Chien PN, Nam SY, Heo CY Int J Mol Sci 24-Aug-2022
PMCID:PMC9455684
doi:10.3390/ijms23179573
PMID:36076971
Putting small and big pieces together: a genome assembly approach reveals the largest Lamiid plastome in a woody vine Fonseca LH, Nazareno AG, Thode VA, Zuntini AR, Lohmann LG PeerJ 07-Apr-2022
PMCID:PMC8995027
doi:10.7717/peerj.13207
PMID:35415013
Green Metallic Nanoparticles: Biosynthesis to Applications Chopra H, Bibi S, Singh I, Hasan MM, Khan MS, Yousafi Q, Baig AA, Rahman MM, Islam F, Emran TB, Cavalu S Front Bioeng Biotechnol 06-Apr-2022
PMCID:PMC9019488
doi:10.3389/fbioe.2022.874742
PMID:35464722
Prevalence of mycorrhizae in host plants and rhizosphere soil: A biodiversity aspect Islam M, Al-Hashimi A, Ayshasiddeka M, Ali H, El Enshasy HA, Dailin DJ, Sayyed RZ, Yeasmin T PLoS One 31-Mar-2022
PMCID:PMC8970520
doi:10.1371/journal.pone.0266403
PMID:35358287
Comparative Analysis of Chloroplast Genome Structure and Phylogenetic Relationships Among Six Taxa Within the Genus Catalpa (Bignoniaceae) Li F, Liu Y, Wang J, Xin P, Zhang J, Zhao K, Zhang M, Yun H, Ma W Front Genet 16-Mar-2022
PMCID:PMC8966708
doi:10.3389/fgene.2022.845619
PMID:35368674
Traditional uses of wild and tended plants in maintaining ecosystem services in agricultural landscapes of the Eastern Cape Province in South Africa Maroyi A J Ethnobiol Ethnomed 15-Mar-2022
PMCID:PMC8925170
doi:10.1186/s13002-022-00512-0
PMID:35292046

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,6S,7R,7aR)-4a,6-dihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde 154497557 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1021/NP50027A003
(1S,4aR,6S,7R,7aR)-4a,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde 101701631 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 101701633 Click to see 522.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 101701632 Click to see 536.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] (E)-3-phenylprop-2-enoate 101599956 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 4-hydroxybenzoate 101701634 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C4=CC=C(C=C4)O 496.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 4-methoxybenzoate 101701635 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C4=CC=C(C=C4)OC 510.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 4-hydroxybenzoate 163023986 Click to see 496.50 unknown https://doi.org/10.1021/NP50027A003
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 162883369 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O 522.50 unknown https://doi.org/10.1021/NP50027A003
[(1S,4aR,6S,7R,7aR)-4-formyl-4a-hydroxy-7-methyl-1-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 162923592 Click to see 536.50 unknown https://doi.org/10.1021/NP50027A003
[4-formyl-4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 3-(4-hydroxyphenyl)prop-2-enoate 78410083 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)O 522.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[4-formyl-4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 3-(4-methoxyphenyl)prop-2-enoate 78410334 Click to see 536.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[4-formyl-4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 3-phenylprop-2-enoate 78410085 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 506.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[4-formyl-4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 4-hydroxybenzoate 78178183 Click to see CC1C(CC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C4=CC=C(C=C4)O 496.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
[4-formyl-4a-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-yl] 4-methoxybenzoate 162966781 Click to see 510.50 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
4a,6-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde 163099253 Click to see 376.36 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
2,6,10,14,19,23,27,31-Octamethyl 2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene 3977 Click to see 536.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1269915/
Lycopene 446925 Click to see 536.90 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1269915/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-[2-(beta-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one 14353406 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
4-hydroxy-4-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]cyclohexan-1-one 11045420 Click to see C1CC(CCC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 320.34 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
4-Hydroxy-4-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]cyclohexan-1-one 14311126 Click to see C1CC(CCC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 320.34 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
CID 11809239 11809239 Click to see C1=CC(C=CC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
Cornoside 3084796 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
> Organoheterocyclic compounds / Benzofurans
Halleridone 146831 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1016/S0031-9422(96)00756-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.14233/AJCHEM.2019.21530
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.14233/AJCHEM.2019.21530
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-O-glucuronide 5319484 Click to see 446.40 unknown https://doi.org/10.14233/AJCHEM.2019.21530
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.14233/AJCHEM.2019.21530
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.14233/AJCHEM.2019.21530

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